"Quest Diagnostics Nichols Institute San Juan Capistrano"[submitter] A - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685895	GRCh37/hg19 3p26.3-24.1(chr3:310747-28297447)x3	ANKRD28, ARL8B +121 more	Copy number gain	not provided	GPathogenic
Select item 2685072	GRCh37/hg19 3p24.3(chr3:17277016-17473530)x1	TBC1D5	Copy number loss	not provided	GUncertain significance
Select item 1808686	GRCh37/hg19 3p24.3(chr3:17311429-17406724)x1	TBC1D5	Copy number loss	not provided	GUncertain significance
Select item 814423	GRCh37/hg19 3p24.3(chr3:17498477-18077057)x3	TBC1D5	Copy number gain	not provided	GUncertain significance
Select item 562761	GRCh37/hg19 3p24.3(chr3:17473055-17629675)x1	TBC1D5	Copy number loss	not provided	GUncertain significance
Select item 562760	GRCh37/hg19 3p24.3-21.31(chr3:16923595-45249923)x2,3	ABHD5, ACAA1 +135 more	Copy number gain	not provided	GPathogenic
Select item 562726	GRCh37/hg19 3p26.3-24.3(chr3:1897972-19519085)x3	ANKRD28, ARL8B +98 more	Copy number gain	not provided	GPathogenic

ClinVar